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Reporte zur Charge U 7452AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

8Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
UT 2 NY 1 OR 1 MO 1 MN 1 VA 1 TX 1

VAERS 2722262

SANOFI PASTEUR · DTAP + IPV (QUADRACEL) · Charge U7452AA

mild
Staat
NY
Alter
6,0
Geschlecht
F
Eingang
08.12.2023
Impfdatum
01.12.2023
Beginn
01.12.2023
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Axillary pain Injection site erythema Injection site reaction Injection site swelling Pain

Symptomtext

Local injection site reaction. Localized reaction at injection site. Redness encompassing right shoulder and deltoid area, swelling noted right upper arm deltoid, pain radiating from right shoulder to right deltoid and right axillary areas. Patient with pain on movement and use of right arm. Reaction started within 2 hours of injection lasting 4-5 days.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Axillary pain
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2680313

SANOFI PASTEUR · DTAP + IPV (QUADRACEL) · Charge U7452AA

mild
Staat
OR
Alter
5,0
Geschlecht
F
Eingang
07.09.2023
Impfdatum
06.09.2023
Beginn
06.09.2023
Tage bis Beginn
0,0
Dosis
5
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Hypersensitivity Injection site reaction Rash Swelling face Urticaria Wheezing

Symptomtext

Patient received scheduled childhood izs @ 1100 9/6/23. Had allergic reaction @ 150 9/6/23; presented to my office with left thigh site reaction, diffuse rash with hives (head to toe), facial swelling, and wheezing. No strider or airway compromise, VS WNL. Tx with 25mg IM Benadryl, 5mg PO Dexamethasone, and 0.5ml 2.25/ racepinephrine neb. Monitored & DC home with Rx for prednisone taper, epipen jr, & OTC Benadryl.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site reaction
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2720213

SANOFI PASTEUR · DTAP + IPV (QUADRACEL) · Charge U 7452AA

gering
Staat
MO
Alter
4,0
Geschlecht
M
Eingang
01.12.2023
Impfdatum
29.11.2023
Beginn
30.11.2023
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Muscle swelling Pallor Peripheral swelling Skin induration

Symptomtext

24 hours after, noticed swelling over the entire right tricep that progressed to 48 hours after. Skin was red, blanching, indurated.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Benadryl for symptoms
Allergien
None
Vorherige Impfungen
-

VAERS 2713561

SANOFI PASTEUR · DTAP + IPV (QUADRACEL) · Charge U7452AA

gering
Staat
MN
Alter
1,3
Geschlecht
F
Eingang
14.11.2023
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product administered to patient of inappropriate age

Symptomtext

administered Quadracel to an underage patient with no reported adverse event; Initial information received on 01-Nov-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 15 months old female patient was administered Diphtheria-15/Tetanus/5 Hybrid Ac Pertussis/Ipv (Mrc5) Vaccine [Quadracel] with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received an 0.5 ml total (1X) of suspect Diphtheria-15/Tetanus/5 Hybrid Ac Pertussis/Ipv (Mrc5) Vaccine Suspension for injection (lot number: U7452AA) (expiry date: 29-Jun-2024) (Frequency: once) via unknown route in unknown administration site for immunization. On an unknown date, the patient was administered Diphtheria-15/Tetanus/5 Hybrid Ac Pertussis/Ipv (Mrc5) Vaccine with no reported adverse event (product administered to patient of inappropriate age) (latency: same day). It was reported, A clinical director of operations reported that they have invertedly administered Quadracel to an underage patient and would like to know what to do moving forward. She said that she saw an article (abbreviation meaning not known) CDC (abbreviation meaning not known) from 2015 that if an underage patient was administered Quadracel, that dose would be counted. She would like to know to know what information we have in regards to this. This situation is reported as a medication error. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2712085

SANOFI PASTEUR · DTAP + IPV (QUADRACEL) · Charge U7452AA

gering
Staat
VA
Alter
1,4
Geschlecht
M
Eingang
09.11.2023
Impfdatum
13.10.2023
Beginn
13.10.2023
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Wrong product administered

Symptomtext

Patient was administered Quadracel vaccine in error. Verbal order was given by the provider. Patient should have received DTap only per vaccine schedule.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Wrong product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2697588

SANOFI PASTEUR · DTAP + IPV (QUADRACEL) · Charge u7452aa

gering
Staat
UT
Alter
11,0
Geschlecht
F
Eingang
17.10.2023
Impfdatum
17.10.2023
Beginn
17.10.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product administered to patient of inappropriate age Wrong product administered

Symptomtext

Erroneous vaccine given for age. Vaccine later approved by pharmacist

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2696474

SANOFI PASTEUR · DTAP + IPV (QUADRACEL) · Charge U7452AA

gering
Staat
TX
Alter
2,0
Geschlecht
M
Eingang
16.10.2023
Impfdatum
01.10.2023
Beginn
01.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Product administered to patient of inappropriate age

Symptomtext

Patient was administered Quadracel and is only 2 years old. Patient should have re two separate vaccines. 1 DTap and 1 IPV. Patient have no adverse reaction to the Quadracil vaccine. Patient tolerated the injection well. Patient and parent was informed by the provider of medication error.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
No
Vorgeschichte
No
Andere Medikamente
N/A
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2665658

SANOFI PASTEUR · DTAP + IPV (QUADRACEL) · Charge U7452AA

gering
Staat
UT
Alter
5,0
Geschlecht
F
Eingang
03.08.2023
Impfdatum
01.08.2023
Beginn
01.08.2023
Tage bis Beginn
0,0
Dosis
5
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Wrong product administered

Symptomtext

Client recieved Twinrix by mistake No reported side effects Unable to reach parent via phone

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
client received Twinrix by mistake
Allergien
none
Vorherige Impfungen
-